期刊
CORONARY ARTERY DISEASE
卷 24, 期 4, 页码 303-311出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MCA.0b013e3283608c32
关键词
Ga-68; myocardial infarction; PET; RGD peptide; therapeutic angiogenesis
资金
- Korea Healthcare Technology R&D Project, Ministry of Health & Welfare, Republic of Korea [A090633]
- Korea Health Promotion Institute [A090633] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
Objective Ga-68-NOTA-RGD PET is a newly developed molecular imaging for angiogenesis. In this study, Ga-68-NOTA-RGD PET was used to investigate imaging characteristics in a rat myocardial infarction (MI) model and to monitor the efficacy of an angiogenesis induction therapy. Materials and methods Ga-68-NOTA-RGD PET was performed serially in rats with MI or sham operation, and myocardial uptake was analyzed with respect to time duration and tissue characteristics. Subsequently, Ga-68-NOTA-RGD PET was serially performed for therapeutic efficacy monitoring in MI-induced rats, which were treated with basic fibroblast growth factor (bFGF) injection or saline injection. Image findings were compared with the final change in MI lesion. Results Ga-68-NOTA-RGD uptake was significantly increased in MI lesion and gradually decreased over time. Ga-68-NOTA-RGD uptake in the infarcted tissue corresponded with vascular endothelial growth factor expression and macrophage accumulation. In monitoring of therapeutic efficacy, the lesion uptake in the bFGF-injected group was significantly higher than that of the saline-injected and sham-operated groups on the first day. However, no significant differences were observed between bFGF and saline-injected groups at subsequent time points, corresponding to the final infarct size change. Conclusion Ga-68-NOTA-RGD PET would be a useful angiogenesis imaging modality in MI for assessment of pathophysiology or monitoring of therapeutic efficacy. Coron Artery Dis 24:303-311 (c) 2013 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据